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1.
Bulletin of Alexandria Faculty of Medicine. 2006; 42 (3): 619-624
en Inglés | IMEMR | ID: emr-172782

RESUMEN

The aim of the present study was to assess the diagnostic value of Cyfra 21-1, CA 19-9 and CEA in serum and bile of patients with CCA. The present study was conducted on 20 patients with cholangiocarcinoma [CCA group] diagnosed on clinical and pathological grounds, in addition to 20 cases with benign cholestatic disorder and 20 matched healthy subjects as a control group. Cyfra 2 1-1, CEA and CA 19-9 were measured in serum and bile of patients and in serum of controls. Serum CEA, CA 19-9 and Cyfra 21-1 concentrations were significantly higher in patients with cholangiocarcinoma than patients with benign cholestatic disorder and controls. Moreover, the mean bile .concentrations of CEA, CA 19-9 and Cyfra 21-1 were significantly higher than serum concentrations. The sensitivity, specificity and diagnostic accuracy of serum and bile Cyfra 21-1 were significantly higher than those obtained using either CEA or CA 19-9. The serum and bile concentrations of CEA, CA 19-9 and Cyfra 21-1 were significantly higher in late stages of CCA in comparison to early stages. The addition of tumor markers CEA, CA l9-9 and Cyfra 21-1 to brush cytology increases its sensitivity in diagnosis of cholangiocarcinoma from 44% up to 84%. CEA, CA 19-9 and Cyfra 21-1 measurements in bile are important for the supplementary diagnosis of cholangiocarcinoma. Cyfra 21-1 is a superior tumor marker than CEA in diagnosis cholangiocarcinoma. Combining brush cytology with CEA, CA 19-9 and Cyfra 21-1 can raise the diagnostic yield


Asunto(s)
Humanos , Masculino , Femenino , Antígenos de Neoplasias/sangre , Antígeno Carcinoembrionario/sangre , Bilis/inmunología , Biomarcadores de Tumor/análisis
2.
Journal of the Egyptian Society of Parasitology. 2002; 32 (3): 987-1002
en Inglés | IMEMR | ID: emr-59757

RESUMEN

To explore the role of Schistosoma mansoni infection in the prevention of autoimmune mediated insulin-dependent diabetes mellitus, the study examined the effects of multiple low doses of the pancreatic islets beta cell toxin, streptozotocin STZ [40 mg/kg] body weight i.p., given eight weeks post infection period of S. mansoni egg deposition on S. mansoni infected C57BL/6J mice in comparison to non-infected STZ given group. G IV was the control group. Mice treated with STZ [G III] became gradually hyperglycemic reaching the highest level on day 17 post STZ. S. Mansoni infection [G II] significantly reduced the elevation in blood glucose levels from day seven post STZ onwards. Morphologic examination of pancreas on day 21 post STZ revealed that the non-infected STZ [G III] given mice had significantly smaller mean islets area and significantly fewer mean number of beta cells/islets. Pancreatic tissue revealed also focal degeneration in the cells of islets of Langerhans in the non-infected STZ given mice [G III] in comparison to the infected STZ given group [G II], which had much less evident cells degeneration


Asunto(s)
Animales de Laboratorio , Autoinmunidad , Tolerancia Inmunológica , Ratones , Diabetes Mellitus Experimental , Estreptozocina , Diabetes Mellitus Tipo 1 , Recuento de Huevos de Parásitos , Esquistosomiasis mansoni
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